Enthalpy

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Enthalpy

For any system, that is, the volume of substance under discussion, enthalpy is the sum of the internal energy of the system plus the system's volume multiplied by the pressure exerted by the system on its surroundings. The sum is given the special symbol H primarily as a matter of convenience because this sum appears repeatedly in thermodynamic discussion. Previously, enthalpy was referred to as total heat or heat content, but these terms are misleading and should be avoided. Enthalpy is, from the viewpoint of mathematics, a point function, as contrasted with heat and work, which are path functions. Point functions depend only on the initial and final states of the system undergoing a change; they are independent of the paths or character of the change. For change in enthalpy with pressure or temperature See Thermodynamic principles, Entropy, Thermodynamic processes

McGraw-Hill Concise Encyclopedia of Physics. © 2002 by The McGraw-Hill Companies, Inc.

Enthalpy

A measure of the total heat content within a given sample of air. It is typically used to determine the amount of fresh outside air that can be added to recirculated air for the lowest heating/cooling cost.
Illustrated Dictionary of Architecture Copyright © 2012, 2002, 1998 by The McGraw-Hill Companies, Inc. All rights reserved

enthalpy

[en′thal·pē]
(thermodynamics)
The sum of the internal energy of a system plus the product of the system's volume multiplied by the pressure exerted on the system by its surroundings. Also known as heat content; sensible heat; total heat.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
The following article is from The Great Soviet Encyclopedia (1979). It might be outdated or ideologically biased.

Enthalpy

 

the thermodynamic potential that characterizes the state of a thermodynamic system upon the selection of entropy 5 and pressure p as the principal independent variables (seePOTENTIALS, THERMODYNAMIC and ). Enthalpy is represented as H(S, p, N, xi), where N is the number of particles in the system and xi is the system’s other macroscopic parameter. It is an additive function; that is, the enthalpy of the entire system is equal to the sum of the enthalpies of its component parts. Enthalpy is related to the internal energy U of the system by the equation

(1) H = U + pV

where V is the volume of the system. The total enthalpy differential, given fixed N and xi, has the form

(2) dH = TdS + vdp

From formula (2) it is possible to determine the temperature T and the volume of the system: T = (αH/αS)p and V = (αHp)s. At constant pressure (p = const), the heat capacity of the system cp = (αH/αT)p (seeHEAT CAPACITY). These properties of enthalpy, at p = const, are similar to the properties of internal energy at constant volume:

A minimum enthalpy value corresponds to the equilibrium state of a system given the constancy of S and p. A change in enthalpy (ΔH) is equal to the amount of heat imparted to the system or removed from it at constant pressure, therefore the values of ΔH characterize the heat effects of phase transitions (melting, boiling), chemical reactions, and other processes that occur at constant pressure. Enthalpy is conserved upon the thermal insulation of bodies (at p = const), and therefore it is sometimes called heat content or total heat. The condition for enthalpy conservation underlies, in particular, the theory of the Joule-Thomson effect, which has found important practical applications in the liquation of gases. The term “enthalpy” was proposed by H. KamerlinghOnnes.

D. N. ZUBAREV

The Great Soviet Encyclopedia, 3rd Edition (1970-1979). © 2010 The Gale Group, Inc. All rights reserved.
References in periodicals archive ?
Thermodynamic parameters such as standard free energy change (IG0), Standard enthalpy change (IH0) and standard entropy change (IS0) can be calculated as [16].
The standard enthalpy of formation at temperature T ([DELTA][H.sub.T.sup.o]) was calculated using the values of standard enthalpy of formation at 25[degrees]C ([DELTA][H.sub.o.sup.o]) (CoO = -60.5 kcal/mol, [Fe.sub.2][O.sub.3] = -44.4 kcal/mol, Si[O.sub.2] = -36.8 kcal/mol, Co[Fe.sub.2][O.sub.4] = -541.7 kcal/mol, and [Co.sub.2]Si[O.sub.4] = -55.2 kcal/mol) according to the following equation [35, 36]:
Thermodynamic quantities such as change of standard free energy (G) change of standard enthalpy (H) and change of standard entropy (S) have been calculated in case of each of the binary mixtures.
The approximate standard enthalpy (Ho) may also be estimated through modifying van't Hoff equation as following: equationWhile the standard entropy (So) can be calculated using the following general thermodynamic relation: equationThe already well-known relation of activation energy of viscosity (Ea), which can give support to the above-suggested relations, as represented by following equation [19]: equationTable 1 lists the viscosity () values withtheir related thermodynamic functions for CTAB/SDS mixtures at different temperatures.

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